L-Oral COUGH RELIEF Syrup

Product NDC
73921-029
11-digit product format
739210029
Labeler code
73921
Product ID
73921-029_a64e83c5-282a-4ceb-bd08-be1b8b0c526e
Type
HUMAN OTC DRUG
Nonproprietary name
Dextromethorphan Hydrobromide, Guaifenesin
Dosage form
SYRUP
Route
ORAL
Labeler
GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-04-01
Marketing end
0000-00-00
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
10 mg/5mL; mg/5mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73921-029-042023-02-08C16284748780-1f386c64a-2926-0266-e053-dadaa90a7c1a18745c15-5075-4ead-b93c-f6e53e6dcdaf
73921-029-042023-01-30C16284748780-1f386c64a-2926-0266-e053-dadaa90a7c1a18745c15-5075-4ead-b93c-f6e53e6dcdaf

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73921-029-04739210029041 BOTTLE in 1 CARTON (73921-029-04) > 118 mL in 1 BOTTLE1 bottle2021-04-010000-00-00NoNoCurrent